fidia farmaceutici spa
सिटो उफिसिएल इटालिया - फ़िडिया फ़ार्मासुटिसी एस.पी.ए.
1946 से, फ़िडिया फ़ार्मासुटिसी डॉक्टरों, भागीदारों और रोगियों को एकीकृत, प्रभावी और सुरक्षित उत्पाद और सेवाएँ प्रदान करने के लिए अनुसंधान और विकास के लिए प्रतिबद्ध है।
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Abano Terme (PD), Italy
- Founded
- 1946
- Website
- https://www.fidiapharma.it
- Categories
- फार्मास्युटिकल विनिर्माण, पैकेजिंग एवं मुद्रण आपूर्तियाँ, पूरक और कल्याण
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- operating-permit (green), effective since 2011-08-01 EEA Industrial Emissions Portal (IED), EU-wide permit register
- registered-manufacturer (green), checked 2026-09-17 Ministero della Salute, banca dati e Repertorio dei dispositivi medici
- public-contract-awarded (green), effective since 2026-07-13 TED (Tenders Electronic Daily), EU public procurement award notices यहाँ ठेका मिलना किसी और की जाँच भी साथ लाता है: यूरोपीय संघ और ईईए में सार्वजनिक क्रेता को धोखाधड़ी, भ्रष्टाचार या धनशोधन में दोषी बोलीदाताओं को, और अंतिम निर्णय से कर या सामाजिक अंशदान बकाया पाए गए बोलीदाताओं को बाहर करना अनिवार्य है। Directive 2014/24/EU, Article 57 (exclusion grounds)
- facility-registered (green), checked 2026-09-07 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
- state-aid-sector (green), effective since 2026-06-03 Registro Nazionale degli Aiuti di Stato (rna.gov.it), open data
- vat-valid (green), checked 2026-08-16 VIES (European Commission)
- public-subsidy-received (green), checked 2026-08-25 OpenCoesione (opencoesione.gov.it), open data on project subjects
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- If the goods are paper, board or printed products, EU imports fall under the Deforestation Regulation (EUDR) due-diligence regime; packaging machinery itself does not. European Commission (EUDR)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)
- No public registry exists for certificates of this kind in this sector: conformity is declared by the manufacturer. European Commission: CE marking, manufacturer's conformity assessment